Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877726Generated: November 1, 2026

Pentafluoropropionic acid → HCID 86643203, compound

https://huagongshe.com/reaction/1877726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentafluoropropionic acidHCID 62356—
ReactantHCID 15537423HCID 15537423—
ReactantSodium t-butoxideHCID 23676156—
ReactantN-(2-Methoxyethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamineHCID 71424406—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86643203HCID 86643203—

Reaction Conditions

Temperature150 °C

Reaction Steps

6.56 g (0.03 moles) of N,N-Bis(trimethylsilyl)-2-methoxyethylamine were mixed with 3.14 g (0.02 moles) of 4-(2-methoxyethylamino)-3-penten-2-one. To this mixture was added 4.1 g (0.026 moles) of pentafluoropropionic acid dropwise over 5 minutes with rapid stirring. The mixture darkened and became warm, eventually forming two immiscible layers, and was allowed to stir for 1 hour. 2.5 g (0.0266 moles) of sodium t-butoxide dissolved in 5 ml of tetrahydrofuran was then added dropwise over a five minute period. The mixture warmed and became one liquid phase, which was yellow. The solvent was then removed by vacuum distillation at room temperature, and the product then vacuum distilled out of the resulting residue as a clear liquid by heating>150° C. Yield of MeC(NCH2CHOMe)CHC(HNCH2CH2OMe)Me=3.9 g (91% of theoretical).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08313807B2
Source datasetuspto-grants-2012_11
ORD IDord-ae6bd8f3eb794bbbab8c8530435c4cb3
Source noteuspto-grants-2012_11